Réaction #70484

Équation de réaction

6-((S)-3-methyl-piperazin-1-yl)-nicotinic acid ethyl ester

1,4-dichlorophthalazine

triethyl amine

→

desired compound

Rendement 30.3%

6-[(S)-4-(4-Chloro-phthalazin-1-yl)-3-methyl-piperazin-1-yl]-nicotinic acid ethyl ester

Rendement 30.3%

Solvants

NMP

water

Conditions de réaction

Traitement

1. 1
   AutreReaction
2. 2
   Extractionextracted with EtOAc (3×25 mL)
3. 3
   SéchageThe combined organic fractions are dried over magnesium sulfate
4. 4
   Concentrationconcentrated
5. 5
   Autrepurified by silica gel chromatography (5-50% EtOAc/Heptane)

Mode opératoire

A solution of 6-((S)-3-methyl-piperazin-1-yl)-nicotinic acid ethyl ester (1.0 g, 4.0 mmol, 1 eq), 1,4-dichlorophthalazine (840 mg, 4.2 mmol, 1.05 eq) and triethyl amine (3.9 g, 2.8 mL, 38 mmol, 9.5 eq) in NMP (8 mL) is heated at 100 C for 26 h. Reaction is diluted with water (15 mL) and extracted with EtOAc (3×25 mL). The combined organic fractions are dried over magnesium sulfate, concentrated and purified by silica gel chromatography (5-50% EtOAc/Heptane) to yield the desired compound (500 mg, 30% yield).

Source